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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244338Generated: October 31, 2026

Triethylamine → 4-Methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid (2-oxo-2-thiophen-3-yl-ethyl)-amide

https://huagongshe.com/reaction/1244338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-Amino-1-(thiophen-2-yl)ethan-1-one hydrochlorideHCID 12609833—
Reactant4-Methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acidHCID 21919216—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid (2-oxo-2-thiophen-3-yl-ethyl)-amideHCID 2113705735.2%

Reaction Steps

0.40 g 4-Methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid and 0.25 g 1,1′-carbonyl-diimidazole in 40 ml DMF were stirred at room temperature for 1.5 hours. 0.27 g 2-amino-1-(2-thienyl)ethanone hydrochloride and 0.15 g triethylamine were added and stirring was continued over night at room temperature. 350 ml water was added and the mixture was extracted with ethylacetate. Chromatography on silicagel with ethylacetate/hexane 4:6 yielded 0.20 g (35%) 4-methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid (2-oxo-2-thiophen-3-yl-ethyl)-amide as a yellow solid; MS (ISP): m/e=418 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122545B2
Source datasetuspto-grants-2006_10
ORD IDord-16b351422c144de8931be4f877166dbf
Source noteuspto-grants-2006_10